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						<p>
							<b>D&eacute;partement de G&eacute;n&eacute;tique et de
								Cytog&eacute;n&eacute;tique</b>
						</p>

						<p>
							<h3>Chef du D&eacute;partement</h3>
							Pr A. Brice
						</p>

						<p>
							<h3>Cadre Sup&eacute;rieur de Laboratoire</h3>
							C. Degoud
						</p> 01.42.17.76.89
						</p>
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						<p>
							<h3>Secr&eacute;tariat</h3>
							Marie-Claire Gerval<br /> 01.42.17.76.47<br />
							T&eacute;l&eacute;copie&nbsp;:<br /> 01.42.17.76.18<br />
						</p>

						<p>
							Dr A. AFENJAR (PHC)<br /> Dr C. BELLANNE-CHANTELOT (MCU-PH)<br />
							Dr B. BENYAHIA (PH)<br /> Pr A. BRICE (PU-PH)<br /> Dr C.
							CAZENEUVE (PH)<br /> Dr P. CHARLES (PH)<br /> Dr Ph. CHARRON
							(MCU-PH)<br /> Dr C. COLAS (AHU)<br /> Dr F. COULET (MCU-PH)<br />
							Dr C. DEPIENNE (Attach&eacute;)<br /> Dr A. DURR (PH)<br /> Dr
							D. HERON (PH)<br /> Dr A. JACQUETTE (CCA)<br /> Dr E. LE GUERN
							(MCU-PH)<br /> Dr S. LESOURD (MCU-PH)<br /> Pr F. SOUBRIER
							(PU-PH)<br />
						</p>

						<p>
							<h3>Attach&eacute;s</h3>
							Dr J. FEINGOLD
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					<td colspan=3><p align=center>Paris, le ##DATE##,</td>
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					<td colspan=3><p align=center>M. le Dr ##NEUROLOGIST##,</td>
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					<td></td>
					<td colspan=3><h3>ANALYSE DU GENE ##GENE## (##ALIAS##)</h3></td>
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								<td>Code BADN :
									##CODE1##-##CODE2##-##CODE3##-##CODE4##-##CODE5##</td>
								<td></td>
								<td>R&eacute;f ADN&nbsp;:</td>
								<td></td>
							</tr>
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								<td>N&eacute;e:</td>
								<td></td>
								<td>Nature du pr&eacute;l&egrave;vement:</td>
								<td></td>
							</tr>
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								<td>Pr&eacute;nom :</td>
								<td></td>
								<td>Date de r&eacute;ception :</td>
								<td></td>
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								<td>Date de naissance :</td>
								<td></td>
								<td>Date du pr&eacute;l&egrave;vement:</td>
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					<td></td>
					<td><u>MOTIF DE L&rsquo;ANALYSE</u></td>
					<td>Recherche de mutation dans un cadre de recherche.</td>
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					<td></td>
					<td><u>ANALYSE DE L&rsquo;ADN</u></td>
					<td>##METHOD##</td>
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					<td style="vertical-align: top;"><u>RESULTAT</u></td>
					<td style="vertical-align: top;">&nbsp;- Absence de mutation
						dans le g&egrave;ne SPG4.<br /> &nbsp;- Pr&eacute;sence
						d&rsquo;une mutation typique du g&egrave;ne SPG4 Il s&rsquo;agit
						d&rsquo;une<br /> mutation d&eacute;jà d&eacute;crite.<br />
						&nbsp;- Pr&eacute;sence d&rsquo;une nouvelle mutation du<br />
						g&egrave;ne SPG4 (&nbsp;????). Son absence sur <b>XX</b><br />
						chromosomes de t&eacute;moins est en faveur de son rôle
						pathog&egrave;ne.<br />
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					<td style="vertical-align: top;"><u>COMMENTAIRE</u></td>
					<td style="vertical-align: top;">Monsieur(Madame) <b>XX</b>n&rsquo;est
						pas/est porteur(euse) d&rsquo;une mutation associ&eacute;e à la
						maladie de<br /> ##PATHOLOGIE## de transmission autosomique
						##MODE##. </span>
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							<td></td>
							<td>Pr Alexis BRICE</td>
							<td>Dr Alexandra D&Uuml;RR</td></td>
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